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GeneBe API Showcase

This page demonstrates how to use the GeneBe API to query variant information. The API provides programmatic access to genomic annotations and variant data.

API presented here should be used for checking single variants. If you want to check many variants at once, please use other API endpoints that you will find in the documentation.

Documentation & Advanced Usage

Complete API documentation:docs.genebe.net/docs/api/overview/

Interactive endpoint tester:api.genebe.net/cloud/gb-api-doc/swagger-ui/

Python client for pandas:pypi.org/project/genebe/

Java CLI for VCF files:github.com/pstawinski/genebe-cli

All tools documented at:docs.genebe.net

API Request Examples for Variant: 14-94380948-A-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=14&pos=94380948&ref=A&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "14",
      "pos": 94380948,
      "ref": "A",
      "alt": "C",
      "effect": "missense_variant",
      "transcript": "NM_000295.5",
      "consequences": [
        {
          "aa_ref": "D",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SERPINA1",
          "gene_hgnc_id": 8941,
          "hgvs_c": "c.840T>G",
          "hgvs_p": "p.Asp280Glu",
          "transcript": "NM_000295.5",
          "protein_id": "NP_000286.3",
          "transcript_support_level": null,
          "aa_start": 280,
          "aa_end": null,
          "aa_length": 418,
          "cds_start": 840,
          "cds_end": null,
          "cds_length": 1257,
          "cdna_start": 887,
          "cdna_end": null,
          "cdna_length": 3006,
          "mane_select": "ENST00000393087.9",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_000295.5"
        },
        {
          "aa_ref": "D",
          "aa_alt": "E",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SERPINA1",
          "gene_hgnc_id": 8941,
          "hgvs_c": "c.840T>G",
          "hgvs_p": "p.Asp280Glu",
          "transcript": "ENST00000393087.9",
          "protein_id": "ENSP00000376802.4",
          "transcript_support_level": 1,
          "aa_start": 280,
          "aa_end": null,
          "aa_length": 418,
          "cds_start": 840,
          "cds_end": null,
          "cds_length": 1257,
          "cdna_start": 887,
          "cdna_end": null,
          "cdna_length": 3006,
          "mane_select": "NM_000295.5",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000393087.9"
        },
        {
          "aa_ref": "D",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SERPINA1",
          "gene_hgnc_id": 8941,
          "hgvs_c": "c.840T>G",
          "hgvs_p": "p.Asp280Glu",
          "transcript": "ENST00000355814.8",
          "protein_id": "ENSP00000348068.4",
          "transcript_support_level": 1,
          "aa_start": 280,
          "aa_end": null,
          "aa_length": 418,
          "cds_start": 840,
          "cds_end": null,
          "cds_length": 1257,
          "cdna_start": 1117,
          "cdna_end": null,
          "cdna_length": 3236,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000355814.8"
        },
        {
          "aa_ref": "D",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SERPINA1",
          "gene_hgnc_id": 8941,
          "hgvs_c": "c.840T>G",
          "hgvs_p": "p.Asp280Glu",
          "transcript": "ENST00000393088.8",
          "protein_id": "ENSP00000376803.4",
          "transcript_support_level": 1,
          "aa_start": 280,
          "aa_end": null,
          "aa_length": 418,
          "cds_start": 840,
          "cds_end": null,
          "cds_length": 1257,
          "cdna_start": 1395,
          "cdna_end": null,
          "cdna_length": 1885,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000393088.8"
        },
        {
          "aa_ref": "D",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SERPINA1",
          "gene_hgnc_id": 8941,
          "hgvs_c": "c.840T>G",
          "hgvs_p": "p.Asp280Glu",
          "transcript": "ENST00000404814.8",
          "protein_id": "ENSP00000385960.4",
          "transcript_support_level": 1,
          "aa_start": 280,
          "aa_end": null,
          "aa_length": 418,
          "cds_start": 840,
          "cds_end": null,
          "cds_length": 1257,
          "cdna_start": 1151,
          "cdna_end": null,
          "cdna_length": 1628,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000404814.8"
        },
        {
          "aa_ref": "D",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SERPINA1",
          "gene_hgnc_id": 8941,
          "hgvs_c": "c.840T>G",
          "hgvs_p": "p.Asp280Glu",
          "transcript": "ENST00000437397.5",
          "protein_id": "ENSP00000408474.1",
          "transcript_support_level": 1,
          "aa_start": 280,
          "aa_end": null,
          "aa_length": 418,
          "cds_start": 840,
          "cds_end": null,
          "cds_length": 1257,
          "cdna_start": 1221,
          "cdna_end": null,
          "cdna_length": 3340,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000437397.5"
        },
        {
          "aa_ref": "D",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SERPINA1",
          "gene_hgnc_id": 8941,
          "hgvs_c": "c.840T>G",
          "hgvs_p": "p.Asp280Glu",
          "transcript": "ENST00000440909.5",
          "protein_id": "ENSP00000390299.1",
          "transcript_support_level": 1,
          "aa_start": 280,
          "aa_end": null,
          "aa_length": 418,
          "cds_start": 840,
          "cds_end": null,
          "cds_length": 1257,
          "cdna_start": 1025,
          "cdna_end": null,
          "cdna_length": 3144,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000440909.5"
        },
        {
          "aa_ref": "D",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SERPINA1",
          "gene_hgnc_id": 8941,
          "hgvs_c": "c.840T>G",
          "hgvs_p": "p.Asp280Glu",
          "transcript": "ENST00000448921.5",
          "protein_id": "ENSP00000416066.1",
          "transcript_support_level": 1,
          "aa_start": 280,
          "aa_end": null,
          "aa_length": 418,
          "cds_start": 840,
          "cds_end": null,
          "cds_length": 1257,
          "cdna_start": 1413,
          "cdna_end": null,
          "cdna_length": 3532,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000448921.5"
        },
        {
          "aa_ref": "D",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SERPINA1",
          "gene_hgnc_id": 8941,
          "hgvs_c": "c.840T>G",
          "hgvs_p": "p.Asp280Glu",
          "transcript": "ENST00000449399.7",
          "protein_id": "ENSP00000416354.3",
          "transcript_support_level": 1,
          "aa_start": 280,
          "aa_end": null,
          "aa_length": 418,
          "cds_start": 840,
          "cds_end": null,
          "cds_length": 1257,
          "cdna_start": 1142,
          "cdna_end": null,
          "cdna_length": 1559,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000449399.7"
        },
        {
          "aa_ref": "D",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SERPINA1",
          "gene_hgnc_id": 8941,
          "hgvs_c": "c.840T>G",
          "hgvs_p": "p.Asp280Glu",
          "transcript": "ENST00000402629.1",
          "protein_id": "ENSP00000386094.1",
          "transcript_support_level": 1,
          "aa_start": 280,
          "aa_end": null,
          "aa_length": 359,
          "cds_start": 840,
          "cds_end": null,
          "cds_length": 1080,
          "cdna_start": 874,
          "cdna_end": null,
          "cdna_length": 1450,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000402629.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SERPINA1",
          "gene_hgnc_id": 8941,
          "hgvs_c": "n.840T>G",
          "hgvs_p": null,
          "transcript": "ENST00000489769.1",
          "protein_id": "ENSP00000451525.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": null,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1562,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "nonsense_mediated_decay",
          "feature": "ENST00000489769.1"
        },
        {
          "aa_ref": "D",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SERPINA1",
          "gene_hgnc_id": 8941,
          "hgvs_c": "c.840T>G",
          "hgvs_p": "p.Asp280Glu",
          "transcript": "NM_001002235.3",
          "protein_id": "NP_001002235.1",
          "transcript_support_level": null,
          "aa_start": 280,
          "aa_end": null,
          "aa_length": 418,
          "cds_start": 840,
          "cds_end": null,
          "cds_length": 1257,
          "cdna_start": 1023,
          "cdna_end": null,
          "cdna_length": 3142,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001002235.3"
        },
        {
          "aa_ref": "D",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SERPINA1",
          "gene_hgnc_id": 8941,
          "hgvs_c": "c.840T>G",
          "hgvs_p": "p.Asp280Glu",
          "transcript": "NM_001002236.3",
          "protein_id": "NP_001002236.1",
          "transcript_support_level": null,
          "aa_start": 280,
          "aa_end": null,
          "aa_length": 418,
          "cds_start": 840,
          "cds_end": null,
          "cds_length": 1257,
          "cdna_start": 1337,
          "cdna_end": null,
          "cdna_length": 3456,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001002236.3"
        },
        {
          "aa_ref": "D",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SERPINA1",
          "gene_hgnc_id": 8941,
          "hgvs_c": "c.840T>G",
          "hgvs_p": "p.Asp280Glu",
          "transcript": "NM_001127700.2",
          "protein_id": "NP_001121172.1",
          "transcript_support_level": null,
          "aa_start": 280,
          "aa_end": null,
          "aa_length": 418,
          "cds_start": 840,
          "cds_end": null,
          "cds_length": 1257,
          "cdna_start": 1060,
          "cdna_end": null,
          "cdna_length": 3179,
          "mane_select": null,
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          "biotype": "protein_coding",
          "feature": "NM_001127700.2"
        },
        {
          "aa_ref": "D",
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SERPINA1",
          "gene_hgnc_id": 8941,
          "hgvs_c": "c.840T>G",
          "hgvs_p": "p.Asp280Glu",
          "transcript": "NM_001127701.2",
          "protein_id": "NP_001121173.1",
          "transcript_support_level": null,
          "aa_start": 280,
          "aa_end": null,
          "aa_length": 418,
          "cds_start": 840,
          "cds_end": null,
          "cds_length": 1257,
          "cdna_start": 1356,
          "cdna_end": null,
          "cdna_length": 3475,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001127701.2"
        },
        {
          "aa_ref": "D",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SERPINA1",
          "gene_hgnc_id": 8941,
          "hgvs_c": "c.840T>G",
          "hgvs_p": "p.Asp280Glu",
          "transcript": "NM_001127702.2",
          "protein_id": "NP_001121174.1",
          "transcript_support_level": null,
          "aa_start": 280,
          "aa_end": null,
          "aa_length": 418,
          "cds_start": 840,
          "cds_end": null,
          "cds_length": 1257,
          "cdna_start": 1164,
          "cdna_end": null,
          "cdna_length": 3283,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001127702.2"
        },
        {
          "aa_ref": "D",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SERPINA1",
          "gene_hgnc_id": 8941,
          "hgvs_c": "c.840T>G",
          "hgvs_p": "p.Asp280Glu",
          "transcript": "NM_001127703.2",
          "protein_id": "NP_001121175.1",
          "transcript_support_level": null,
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          "aa_end": null,
          "aa_length": 418,
          "cds_start": 840,
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          "cdna_start": 1319,
          "cdna_end": null,
          "cdna_length": 3438,
          "mane_select": null,
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          "biotype": "protein_coding",
          "feature": "NM_001127703.2"
        },
        {
          "aa_ref": "D",
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SERPINA1",
          "gene_hgnc_id": 8941,
          "hgvs_c": "c.840T>G",
          "hgvs_p": "p.Asp280Glu",
          "transcript": "NM_001127704.2",
          "protein_id": "NP_001121176.1",
          "transcript_support_level": null,
          "aa_start": 280,
          "aa_end": null,
          "aa_length": 418,
          "cds_start": 840,
          "cds_end": null,
          "cds_length": 1257,
          "cdna_start": 1316,
          "cdna_end": null,
          "cdna_length": 3435,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001127704.2"
        },
        {
          "aa_ref": "D",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SERPINA1",
          "gene_hgnc_id": 8941,
          "hgvs_c": "c.840T>G",
          "hgvs_p": "p.Asp280Glu",
          "transcript": "NM_001127705.2",
          "protein_id": "NP_001121177.1",
          "transcript_support_level": null,
          "aa_start": 280,
          "aa_end": null,
          "aa_length": 418,
          "cds_start": 840,
          "cds_end": null,
          "cds_length": 1257,
          "cdna_start": 1334,
          "cdna_end": null,
          "cdna_length": 3453,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001127705.2"
        },
        {
          "aa_ref": "D",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SERPINA1",
          "gene_hgnc_id": 8941,
          "hgvs_c": "c.840T>G",
          "hgvs_p": "p.Asp280Glu",
          "transcript": "NM_001127706.2",
          "protein_id": "NP_001121178.1",
          "transcript_support_level": null,
          "aa_start": 280,
          "aa_end": null,
          "aa_length": 418,
          "cds_start": 840,
          "cds_end": null,
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      "allele_count_reference_population": 0,
      "gnomad_exomes_af": null,
      "gnomad_genomes_af": null,
      "gnomad_exomes_ac": null,
      "gnomad_genomes_ac": null,
      "gnomad_exomes_homalt": null,
      "gnomad_genomes_homalt": null,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": 0.20970770716667175,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "MetaRNN",
      "splice_score_selected": 0,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": 0.215,
      "revel_prediction": "Benign",
      "alphamissense_score": 0.2327,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.44,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -0.771,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0,
      "spliceai_max_prediction": "Benign",
      "dbscsnv_ada_score": null,
      "dbscsnv_ada_prediction": null,
      "apogee2_score": null,
      "apogee2_prediction": null,
      "mitotip_score": null,
      "mitotip_prediction": null,
      "acmg_score": 4,
      "acmg_classification": "Uncertain_significance",
      "acmg_criteria": "PM1,PM2,PM5,BP4_Moderate",
      "acmg_by_gene": [
        {
          "score": 4,
          "benign_score": 2,
          "pathogenic_score": 6,
          "criteria": [
            "PM1",
            "PM2",
            "PM5",
            "BP4_Moderate"
          ],
          "verdict": "Uncertain_significance",
          "transcript": "NM_000295.5",
          "gene_symbol": "SERPINA1",
          "hgnc_id": 8941,
          "effects": [
            "missense_variant"
          ],
          "inheritance_mode": "AR,AD",
          "hgvs_c": "c.840T>G",
          "hgvs_p": "p.Asp280Glu"
        }
      ],
      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
  ],
  "message": null
}
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